| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | HOXB-AS3, HOXB6 +1 more (R197Q) | Single nucleotide variant (missense variant) | not specified | |
| | HOXB-AS3, HOXB6 +1 more (P129R) | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (intron variant) | Meckel syndrome, type 1 | |
| | | Single nucleotide variant (synonymous variant) | HOXB6-related disorder | |
| | | Single nucleotide variant (synonymous variant) | HOXB6-related disorder | |
| | | Single nucleotide variant (synonymous variant) | HOXB6-related disorder | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | HOXB-AS3, HOXB6 +1 more (R133Q) | Single nucleotide variant (missense variant) | not specified | |
| | HOXB-AS3, HOXB6 +1 more (A33G) | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | HOXB-AS3, HOXB6 +1 more (L27I) | Single nucleotide variant (missense variant) | not specified | |
| | HOXB-AS3, HOXB6 +1 more (N135K) | Single nucleotide variant (missense variant) | not specified | |
| | HOXB-AS3, HOXB6 +1 more (M134I) | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (3 prime UTR variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (3 prime UTR variant) | not provided | |
| | | Deletion (intron variant) | not provided | |
| | | Single nucleotide variant (3 prime UTR variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (3 prime UTR variant) | not provided | |
| | HOXB-AS3, HOXB6 +1 more (G31S) | Single nucleotide variant (missense variant) | not specified | |
| | LOC130061087, HOXB6 +1 more (G146S) | Single nucleotide variant (missense variant) | not specified | |